NDC 75849-200 Valtrum Us Aerobic Sport Immediate Action
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75849 - Laboratorios Quantium Llc
- 75849-200 - Valtrum Us Aerobic Sport Immediate Action
Product Packages
NDC Code 75849-200-00
Package Description: 118 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 75849-200?
What are the uses for Valtrum Us Aerobic Sport Immediate Action?
Which are Valtrum Us Aerobic Sport Immediate Action UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Valtrum Us Aerobic Sport Immediate Action Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ARNICA MONTANA (UNII: O80TY208ZW)
- CAT'S CLAW (UNII: 9060PRM18Q)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Valtrum Us Aerobic Sport Immediate Action?
- RxCUI: 1426990 - camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % Topical Spray
- RxCUI: 1426990 - camphor 25 MG/ML / menthol 25 MG/ML / methyl salicylate 100 MG/ML Topical Spray
- RxCUI: 1426992 - Valtrum Sport 2.5 % / 2.5 % / 10 % Topical Spray
- RxCUI: 1426992 - camphor 25 MG/ML / menthol 25 MG/ML / methyl salicylate 100 MG/ML Topical Spray [Valtrum Sport]
- RxCUI: 1426992 - Valtrum Soothing (camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % ) Topical Spray
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".